HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99420604C= , CM000666.2:g.99420604C= | GRCh38 |
NC_000004.11:g.100341761C= , CM000666.1:g.100341761C= | GRCh37 |
NC_000004.10:g.100560784C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437033.7:c.754G= MANE Select | ENSP00000414254.2:p.Glu252= | |
ENST00000209665.8:c.790G= | ENSP00000209665.4:p.Glu264= | |
ENST00000437033.6:c.754G= | ENSP00000414254.2:p.Glu252= | |
ENST00000476959.5:c.814G= | ENSP00000420269.1:p.Glu272= | |
ENST00000482593.5:c.583G= | ENSP00000420613.1:p.Glu195= | |
NM_000673.4:c.790G= | NP_000664.2:p.Glu264= | |
NM_001166504.1:c.814G= | NP_001159976.1:p.Glu272= | |
NM_000673.7:c.754G= MANE Select | NP_000664.3:p.Glu252= | |
NM_001166504.2:c.814G= | NP_001159976.1:p.Glu272= |